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The French National Registry of patients with Facioscapulohumeral muscular dystrophy
BACKGROUND: Facioscapulohumeral muscular dystrophy is a rare inherited neuromuscular disease with an estimated prevalence of 1/20,000 and France therefore harbors about 3000 FSHD patients. With research progress and the development of targeted therapies, patients’ identification through registries c...
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| Veröffentlicht in: | Orphanet J Rare Dis |
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| Hauptverfasser: | , , , , , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
BioMed Central
2018
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6280451/ https://ncbi.nlm.nih.gov/pubmed/30514324 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13023-018-0960-x |
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